Schott JJ - Search Results

1

Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block.

Syam N, Chatel S, Ozhathil LC, Sottas V, Rougier JS, Baruteau A, Baron E, Amarouch MY, Daumy X, Probst V, Schott JJ, Abriel H. Syam N, et al. Among authors: schott jj. J Am Heart Assoc. 2016 May 20;5(5):e001625. doi: 10.1161/JAHA.114.001625. J Am Heart Assoc. 2016. PMID: 27207958 Free PMC article.

2

Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28.

Trochu JN, Kyndt F, Schott JJ, Gueffet JP, Probst V, Bénichou B, Le Marec H. Trochu JN, et al. Among authors: schott jj. J Am Coll Cardiol. 2000 Jun;35(7):1890-7. doi: 10.1016/s0735-1097(00)00617-3. J Am Coll Cardiol. 2000. PMID: 10841240 Free article.

3

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease.

Probst V, Kyndt F, Potet F, Trochu JN, Mialet G, Demolombe S, Schott JJ, Baró I, Escande D, Le Marec H. Probst V, et al. Among authors: schott jj. J Am Coll Cardiol. 2003 Feb 19;41(4):643-52. doi: 10.1016/s0735-1097(02)02864-4. J Am Coll Cardiol. 2003. PMID: 12598077 Free article.

4

Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype.

Probst V, Allouis M, Kyndt F, Lande G, Trochu JN, Schott JJ, Le Marec H. Probst V, et al. Among authors: schott jj. Am J Cardiol. 2003 Mar 1;91(5):635-7. doi: 10.1016/s0002-9149(02)03329-5. Am J Cardiol. 2003. PMID: 12615283 No abstract available.

5

Novel brugada SCN5A mutation leading to ST segment elevation in the inferior or the right precordial leads.

Potet F, Mabo P, Le Coq G, Probst V, Schott JJ, Airaud F, Guihard G, Daubert JC, Escande D, Le Marec H. Potet F, et al. Among authors: schott jj. J Cardiovasc Electrophysiol. 2003 Feb;14(2):200-3. doi: 10.1046/j.1540-8167.2003.02382.x. J Cardiovasc Electrophysiol. 2003. PMID: 12693506

6

[Genetics and cardiac arrhythmias].

Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1054-62. Arch Mal Coeur Vaiss. 2003. PMID: 14694781 Review. French.

7

[Genetic aspects of cardiac conduction defects].

Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1067-73. Arch Mal Coeur Vaiss. 2003. PMID: 14694782 Review. French.

8

Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation.

Allouis M, Probst V, Jaafar P, Schott JJ, Le Marec H. Allouis M, et al. Among authors: schott jj. Am J Cardiol. 2005 Mar 1;95(5):700-2. doi: 10.1016/j.amjcard.2004.10.057. Am J Cardiol. 2005. PMID: 15721128

9

Monomorphic ventricular tachycardia due to Brugada syndrome successfully treated by hydroquinidine therapy in a 3-year-old child.

Probst V, Evain S, Gournay V, Marie A, Schott JJ, Boisseau P, LE Marec H. Probst V, et al. Among authors: schott jj. J Cardiovasc Electrophysiol. 2006 Jan;17(1):97-100. doi: 10.1111/j.1540-8167.2005.00329.x. J Cardiovasc Electrophysiol. 2006. PMID: 16426410

10

Familial aggregation of calcific aortic valve stenosis in the western part of France.

Probst V, Le Scouarnec S, Legendre A, Jousseaume V, Jaafar P, Nguyen JM, Chaventré A, Le Marec H, Schott JJ. Probst V, et al. Among authors: schott jj. Circulation. 2006 Feb 14;113(6):856-60. doi: 10.1161/CIRCULATIONAHA.105.569467. Epub 2006 Feb 6. Circulation. 2006. PMID: 16461814

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

150 results

Search Page

Filters